Skip to content

I-Dent

IsraelFDA 510(k) applicant, unverified

Devices
1

What I-Dent makes

I-Dent manufactures dental implants, including the IMPLANTMASTER system, designed for surgical placement in the jawbone to support prosthetic teeth or dental restorations.

The company’s products are classified as Class II medical devices under FDA regulations and are listed via the 510(k) pathway. The manufacturer operates from the United States.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Implantmaster Ref K042212

    Class II
    Active 510(k) 510(k) II

Frequently asked questions

How many devices does I-Dent have in the registry?

The registry currently lists 1 device for I-Dent. Devices recorded under merged duplicate company entries are counted once.

Which registries list I-Dent's devices?

Among its 1 most recently registered device, I-Dent has devices listed in FDA 510(k) (1 device).

What risk classes do I-Dent's devices fall under?

Among its 1 most recently registered device, the classes recorded for I-Dent's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from I-Dent in the registry?

The most recently registered devices listed for I-Dent include IMPLANTMASTER.

Generated automatically from registry data and not verified by a human reviewer.